| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:71663807-71664545 | Common:1; Rare:212 | ||||
| chr12:71686014-71686120 | Common:1; Rare:28 | ||||
| chr12:71839602-71839806 | Common:1; Rare:80 | ||||
| chr12:74537707-74537890 | Common:1; Rare:69 | ||||
| chr12:75209458-75209764 | Common:2; Rare:73 | ||||
| chr12:75330311-75330619 | Rare:82 | ||||
| chr12:75390870-75391211 | Common:1; Rare:122 | ||||
| chr12:75511578-75511844 | Rare:80 | ||||
| chr12:76084569-76084799 | Common:1; Rare:77 | ||||
| chr12:76084956-76085105 | Common:3; Rare:32 | ||||
| chr12:76348351-76348468 | Common:1; Rare:46; Clinvar:3; Clinvar (benign):1 | ||||
| chr12:76422740-76422837 | Rare:25 | ||||
| chr12:76559502-76559918 | Common:2; Rare:137 | ||||
| chr12:76764051-76764329 | Common:1; Rare:119 | ||||
| chr12:78864577-78865105 | Common:2; Rare:114 |